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At least 955 records · Page 53

Cost Analysis of Wind and Uranium from Seawater Acquisition symbiotic Infrastructure using Shell Enclosures

At current consumption rates, global conventional reserves of uranium, estimated to be 7.6 million tonnes, could be depleted in a little over a century. As these reserves decrease, extraction of uranium is expected to shift to lower quality sites, resulting in higher extraction costs and greater environmental impact. Fortunately, the ocean contains approximately 4.5 billion tonnes of uranium, as uranyl ions at low concentrations of about 3 ppb. Uranium from seawater is a widely studied topic due to the long term security it can assure the nuclear fuel cycle. Additionally, harvesting uranium from seawater could reduce some of the environmental impacts associated with the recovery of land-based uranium. Seawater uranium is meant to create a cost ceiling that provides economic stability and potential savings, not to act as a direct competitor to terrestrial uranium. A recent review of uranium recovery technologies by found uranium adsorption by chelating polymers to be the most promising in terms of adsorbent capacity, environmental footprint, and cost. In this technology, chelating polymers are deployed in seawater and remain submerged until the amount of captured uranium approaches the adsorption capacity. Then, an elution bath is used to strip metal ions, such as uranium, off the adsorbent polymer. A polymer may be immersed in a number of elution baths before it is regenerated by an alkali wash to free its functional groups, allowing for the reuse of the polymer. The output from the elution process undergoes purification and precipitation typical for mined uranium to produce yellowcake. Offshore systems for the extraction of uranium from seawater have been developed since the early 2000's. The system currently studied by a nationwide consortium of national laboratory and university partners utilizes continuous adsorbent polyethylene fibers that are braided around a porous polypropylene float which can be made into long lengths. However, because this deployment scheme requires the adsorbent be brought to a mother-ship for the elution process and redeployed afterward, it has significant practical and economic deployment challenges. Detailed economic analysis have identified the adsorbent production and mooring as the most expensive components of the recovery process. Based on these results, proposed an alternative deployment method that is attached to an offshore wind turbine and continuously takes the adsorbent, that is fabricated into a belt, from the ocean through an elution process and before submerging it back into the sea. However, it has been found that adsorbents with high tensile strength and durability often have very low uranium adsorption properties. Hence, the Wind and Uranium from Seawater Acquisition symbiotic Infrastructure (WUSABI) previously studied, which requires the adsorbent into a belt held in tension, could face difficulties in an ocean environment. Instead, the design, further referred to in this paper as WUSABI-Koosh, utilized a two-part system to decouple the mechanical and chemical needs of an adsorbent for seawater harvesting of uranium. In these designs, the uranium adsorbent material with high adsorbent capacity is enclosed in a hard permeable outer shell with sufficient mechanical strength and durability for use in an offshore environment and chemical resilience against elution treatments. The integration of the design of a uranium harvesting system into an offshore wind turbine tower is pursued because the development of offshore wind or uranium harvesting by themselves bears a high capital cost for the structures, but if the mooring function can be shared, the overall cost for each will be lower. Furthermore, initial design analysis and prototyping of these symbiotic systems has proven they are technically feasible. This paper presents preliminary cost analysis for comparison to uranium recovery via alternative deployment schemes.

07 ISOTOPE AND RADIATION SOURCES↗

High surface area Pd nanocatalyst on core-shell tungsten based support as a beneficial catalyst for low temperature fuel cells application

In this paper, tungsten based support was prepared by polycondensation of resorcinol and formaldehyde from ammonium metatungstate, in the presence cetyltrimethylammonium bromide (CTABr) surfactant. Pd nanocatalyst on this support was synthesized by borohydride reduction method. The obtained materials were characterized by High Resolution Transmission Electron Microscopy (HRTEM), Electron Energy Loss Spectroscopy (EELS), X-ray Photoelectron Spectroscopy (XPS) and electrochemical measurements. TEM analysis revealed Pd nanoparticles size in the range of a few nanometers, even the clusters of single Pd atoms. X-Ray Photoelectron Spectroscopy was applied to determine surface composition of the substrates. It was found that tungsten based support consisted of W, WC and WO 3 species. The presence of metallic palladium – Pd(0) in the Pd/W@WCWO 3 catalyst was revealed, as well. The catalytic activity and stability for the oxygen reduction were investigated in acid and alkaline solutions, by cyclic voltammetry and linear sweep voltammetry at the rotating disc electrode. The catalysts' activities were compared to the carbon supported Pd nanoparticles (Vulcan XC 72). Finally, WC supported Pd nanoparticles have shown high activity and superior stability, comparable even to Pt based catalysts, especially in alkaline electrolytes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Effect of Ce addition on the microstructure and properties of Al-Cu-Mn-Mg-Fe lithium battery shell alloy

Highlights: • Al{sub 6}(Mn, Fe) particles could be remarkably refined by Ce alloying. • Ce addition to the alloy promoted precipitation of S' phase. • Ce-containing alloy had higher tensile strength than that of Ce-free alloy. • Ce-containing alloy had positive corrosion potential and lower corrosion current density. - Abstract: Effect of Ce addition on the microstructures, mechanical properties and electrochemical properties of Al-Cu-Mn-Mg-Fe lithium battery alloy was investigated by optical microscope (OM), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), tensile testing and electrochemical testing. Experimental results indicate that Ce addition resulted in the formation of Al{sub 8}Cu{sub 4}Ce phase in the Al-Cu-Mn-Mg-Fe alloy. The Ce-containing precipitates nucleated and grew up along the surface of Al{sub 6}(Mn, Fe) precipitates. Al{sub 6}(Mn, Fe) precipitates could be remarkably refined by Ce alloying. The aging precipitation behavior of S' phases could be promoted after Ce addition to the alloy. In comparison with Ce-free alloy, the Ce-containing alloy had higher tensile strength at both low temperature and elevated temperature. Especially at 200 °C, the yield strength and tensile strength of Ce-containing alloy substantially increased by 23.4% and 27.08%, respectively. Potentiodynamic polarization testing indicated that the Ce-containing alloy had a more positive corrosion potential and a lower corrosion current density.

36 MATERIALS SCIENCE↗

Enhanced long-term cyclability in Li-Rich layered oxides by electrochemically constructing a Li x TM 3-x O 4 -type spinel shell

The poor long-term cycling stability, including the fast capacity fade and the severe voltage decay, has become the main concern hindering the practical application of Li-rich layered oxides, a promising cathode for high- energy-density Li-ion battery. Herein, we design and electrochemically construct a ~10 nm-thick Li x TM 3-x O 4 - type (TM ¼Ni, Co, Mn, 0 3 O 4 -type spinel phase and the good Liþconductivity of LiMn 2 O 4 -type spinel phase. Systemic structural and electrochemical analysis demonstrate that, it slows down the activation rate of Li 2 MnO 3 component and efficiently alleviates the lattice O loss at high voltage (>4.5 V) and Mn dissolution, thereby suppressing the structural degradation from the layered phase to the spinel phase in the bulk, eventually significantly enhancing the long-term cycling stability. This study adds richness into the Mn-based spinel phase system and provides a new heterostructure design strategy to improve the electrochemical performance of Li-rich layered cathodes and beyond.

25 ENERGY STORAGE↗

Helium partitioning to the core-shelled Ta nanoclusters in nanocrystalline Cu-Ta alloy

In this work, a nanocrystalline (NC) Cu-10at.%Ta alloy is irradiated with helium at different temperatures to assess the stability and effectiveness of Ta nanoclusters in trapping helium and suppressing swelling. Advanced microstructural characterization of the room-temperature irradiated specimens indicated the presence of small He-bubbles (∼1-2 nm) at the peak damage depth mainly at the core and along the interface of Ta nanoclusters with Cu matrix. Few bubbles were found along grain boundaries, with much smaller bubbles homogenously distributed within the copper lattice. High-temperature irradiation exhibited bubbles of ∼3-5 nm, which were primarily associated with nanoclusters as compared to other locations, with no observed faceting of the bubbles. In conclusion, atom probe analysis confirmed helium partitioning to the Ta nanoclusters indicating the effective entrapment of these He atoms.

36 MATERIALS SCIENCE↗

Discerning structure sensitivity of Ni-core Pd-shell nanoparticles for enhanced nitrite reduction

Denitrification using Pd-based catalysts converts N-oxyanions into harmless products. However, the metal cost and scarcity are barriers to application. In this work, we synthesize water-suspended, structure-controlled Ni-core/Pd-shell nanoparticles (Ni@Pd NPs) that show Pd-catalyzed nitrite (NO 2 − ) reduction catalysis promoted by Ni. The NPs immobilized on Al 2 O 3 (0.47 wt % Pd and 0.74 wt % Ni) have higher NH 4 + selectivity and higher catalytic activity than wet-impregnated Pd/Al 2 O 3 (1.0 wt % Pd), i.e., 315.4 vs. 132.1 Lg surface Pd −1 min −1 . X-ray photoelectron spectroscopy (XPS) and CO-diffuse reflectance infrared Fourier transform spectroscopy (CO-DRIFTS) analyses show that Ni increases Pd electron density, which is proposed to lower the bond dissociation energy barrier for nitric oxide surface intermediate. Low-coordinated Pd atoms correlate to high activity and low NH 4 + selectivity. Using CatCost software, we estimate Ni@Pd/Al 2 O 3 to have a ∼40% lower manufacturing cost compared to wet-impregnated Pd/Al 2 O 3 . This rationally designed catalyst illustrates how nickel promotes Pd catalysis and how Pd usage can be lowered for denitrification and other hydrogenation reactions.

CO-DRIFTS↗